Canonical Allele Identifier: PA2827010454
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65296
ClinVar RCV Id: RCV000055518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu1635Pro
CA022298
NM_001318829.2:c.4904T>C